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AGM-212 elicited slightly greater insulin secretion than exenatide in rat islets, which confirmed the strong insulinotropic activity of AGM-212.
AGM-212 which was subcutaneously injected into diabetic mice under non-fasting maintained normoglycemia for more than 40h post-injection.
The pharmacokinetic profiles of AGM-212 exhibited much longer half-life (2.25h) than exenatide (0.47h).